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Research 121–150 of 1000+
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Gene Delivery to the Hair Follicle
- Hair and nail adverse events during treatment with targeted therapies for metastatic melanoma
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Insertional mutation of the hairless locus on mouse Chromosome 14
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Human Hairless Protein Roles in Skin/Hair and Emerging Connections to Brain and Other Cancers
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- An in vivo method for the detection of somatic mutations at the cellular level in mice
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle